28 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HOFFMANN 3 MODULAR EXTERNAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II
ArgenZ Anterior 95x10 #4
FDA UDI
ARGEN CORPORATION, THE·D818121252·Dental porcelain/ceramic restoration kit
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383505734·Gutta Percha Points is used to root canal filin...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970430·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973691·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973073·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970447·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973905·
NEOTRACT ANCHOR SYSTEM MODEL: REF 11208
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BLOOD-PRESSURE METER
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970423·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970393·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970416·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970409·
980 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·December 14, 2016
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·June 20, 2017
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·August 1, 2017
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·July 25, 2017
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·August 17, 2017